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Quality Assurance System Manager

Nexia Life Sciences
Glasgow
2 months ago
Applications closed

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Overview:

This is a senior site-based quality role with responsibility for managing and developing the Quality Management System to ensure full GxP compliance. As QA Systems Manager, you’ll act as a key member of the Quality leadership team and take ownership of site-wide quality processes, with particular focus on data integrity, validation oversight, documentation, and continuous improvement of systems that support GMP/GDP operations.

You’ll also work closely with colleagues across Quality, Validation, Manufacturing, and IT, providing compliance guidance and driving a strong quality culture.


Key Responsibilities:

  • Lead the development, maintenance and ongoing compliance of the site QMS in line with GxP requirements
  • Act as site lead for data integrity, ensuring systems and processes support secure, traceable and compliant data management
  • Oversee the validation master plan and provide QA oversight for validation-related activities across the site
  • Manage and improve key quality systems including change control, CAPA, deviations, document control and training compliance
  • Provide input and quality guidance on GxP-related investigations, audits and continuous improvement initiatives
  • Deliver training and coaching across departments to reinforce best practice in quality and compliance
  • Maintain oversight of system-based metrics and reporting to support inspection readiness and internal performance monitoring
  • Contribute to Quality leadership team projects and initiatives to enhance overall site compliance


Ideal Experience:

  • Extensive experience in pharmaceutical QA, with a strong understanding of GMP and GDP
  • Proven track record in managing QMS elements, including validation, documentation, and data integrity
  • Experience supporting inspections and audits, both internal and external
  • Excellent communication and stakeholder engagement skills across cross-functional teams
  • Familiarity with electronic quality systems (such as LIMS, TrackWise or Documentum) is advantageous
  • Scientific or technical background preferred
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